20 Best Study Manager jobs (Hiring Now!)

Clinical Research Coordinator
CenExel Rocky Mountain Clinical Research —Englewood, CO
CCRC certification not required, but preferred. O Responsible for timely data entry and query resolution. Knowledge of all components of the research process as…
$29 - $32 an hour
Quick Apply
Clinical Project Manager – Senior - Information Services Regional Strategic Projects
Indiana University Health —Indianapolis, IN
Facilitates current and future state clinical processes, requirements, elicitation, solutions and development and test management.
Estimated: $97.9K - $124K a year
Clinical Study Manager (USA - REMOTE)
VivoSense Inc —Boston, MA
This is a multi-faceted role in which you will have the opportunity to lead the scientific offering on client projects including 1) driving all phases of…
$90,000 - $120,000 a year
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17h
Clinical Research Coordinator I Registered Nurse
Novant Health —Charlotte, NC
Licensure/Certification: Current RN licensure in appropriate state, required. Additional Skills (preferred): Good Clinical Practice (GCP), Human Subjects…
Estimated: $57K - $72.2K a year
7d
Senior Clinical Research Coordinator
Evolution Research Group —Staten Island, NY
Manage studies with Principal Investigator, Site Director, and Recruitment Manager to develop effective programs for study enrollment.
$30 - $38 an hour
Quick Apply
13d
Clinical Research Coordinator
Alliance for Multispecialty Research, LLC —Fort Myers, FL
Advise Investigator, Sub-Investigator and staff on protocols, procedures required for the successful implementation and completion of each clinical research…
From $25 an hour
Quick Apply
3d
Clinical Research Coordinator
Alliance for Multispeciality Research —New Orleans, LA
Attach original document to certified copy before filing in the patient’s chart. Advise Investigator, Sub-Investigator and staff on protocols, procedures…
$24 - $27 an hour
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12d
Clinical Research Site Manager
Alliance for Multispeciality Research, LLC —Layton, UT
Hire, train and develop new team members to meet organizational needs. Provide timely feedback on employee performance, helping to develop a team members skill…
$90,000 - $95,000 a year
Quick Apply
4d
Clinical Research Coordinator (CRC)-FT
Evolution Research Group —Columbus, OH
Manage studies with Principal Investigator, Site Director, and Recruitment Manager to develop effective programs for study enrollment.
Estimated: $49.3K - $62.4K a year
Quick Apply
Clinical Study Manager
ProKidney —Boston, MA
Responsible for the global execution of large, complex clinical trials from study design through study close out, working closely with CRO's and trial sites.
Estimated: $115K - $146K a year
Quick Apply
5d
Clinical Research Nurse Coordinator
University of Alabama at Birmingham —Birmingham, AL
Bachelor's degree in a related field and three (3) years of related experience required. May provide oversight to junior clinical research coordinators (CRC)…
Estimated: $54.2K - $68.6K a year
Non-Clinical Study Manager
Astellas —South San Francisco, CA
Understanding of gene therapy and/or novel biologics concepts and methodologies, in particular as they relate to nonclinical study design and data analysis.
$114,800 - $153,000 a year
4h
Senior Clinical Data Manager
Celldex Therapeutics, Inc. —New Haven, CT
Initiate CRF development for new clinical trials and protocol amendments; collaborate with internal team and responsible vendor on CRF development, database…
Estimated: $124K - $157K a year
RN Clinical Research Coordinator
Gundersen Health System —La Crosse, WI
RN license to work in Wisconsin upon hire. Preform nursing assessments to monitor subject’s progress during clinical research trials.
$29.47 - $45.37 an hour
Quick Apply
Study Start Up Manager
Bristol-Myers Squibb —Illinois
For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf…
Estimated: $107K - $135K a year
5d
Clinical Project Manager
Technical Resources International, Inc. —Bethesda, MD
Broad multidisciplinary understanding of the pharmaceutical clinical research and development processes with hands on regulatory, clinical operations, or…
Estimated: $106K - $134K a year
Customer Success Manager, Clinical Trials
H1 —Remote
This Customer Success Manager will own H1’s Trial Landscape offering. You’ll solve business problems, support, and develop relationships with H1’s largest…
$90,000 - $110,000 a year
17h
Looking for Psychiatry Research Coordinator/Sub-Investigator Position
TIME ORGANIZATION, INC —Baltimore, MD
Knowledge of clinical trial phases, research methodologies, and regulatory requirements, including IRB protocols and Good Clinical Practice (GCP) guidelines is…
$25 - $30 an hour
Quick Apply
7d
Clinical Research Coordinator (medical research trial coordinator with 1 year experience)
One of a Kind Clinical Research Center CA LLC —Napa, CA
Data collection, entry, query resolution. Our site is responsible for coordinating a clinical trial start up, participant recruitment, trial management and…
$23 - $25 an hour
Quick Apply
Senior, Clinical Study Manager
Daiichi Sankyo, Inc. —Remote
If assigned, Sr. CSM may act as the Study Team Leader for the assigned clinical study and responsible for leading the cross-functional study team, project…
Estimated: $133K - $168K a year
3d

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Clinical Research Coordinator

CenExel Rocky Mountain Clinical Research - Englewood, CO

Quick Apply

Job Details

Full-time $29 - $32 an hour

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
401(k) matching
Employee discount
Flexible schedule
Life insurance

Qualifications

Microsoft Word
CCRC
Microsoft Excel
Clinical research
Phlebotomy
Clinical trials
Good Clinical Practice
Computer skills
Neurology
1 year
Care plans

Full Job Description

About Us:

Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.

Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

Job Summary:

Responsible for coordinating all aspects of clinical trials with the strictest adherence to ICH, GCP, protocol, and company guidelines, regulations, and policies.

Essential Responsibilities and Duties:

· Coordinating all aspects of patient involvement from study initiation until study completion;

· Study start-up:

· o assist in the creation of thorough and accurate source documents;

· o Work collaboratively with other internal departments, sponsors and investigators to ensure protocols are understood and assist in the trainings of staff members

· o Participate in IMs and SIVs; communicating with sponsors and representatives

· o Ensure site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.)

· Screening participants for actively enrolling studies

· o Assist in reviewing all participant history from Pre-Enrollment and Enrollment departments confirming information with potential participant and study physician

· o Educating potential participants and caregivers on protocol specific details and expectations;

· o Working with the physician to address all questions and concerns related to the trial and informed consent process;

· o Maintaining thorough knowledge of study specific inclusion/exclusion criteria

· Coordinating scheduled visits and adhering to protocol visit windows and timelines

· o Perform or follow up on safety and efficacy assessments per protocol  vital signs, EKGs, blood draws and other assessments as assigned

· o Collaborating with the research pharmacist to perform drug accountability and compliance at each visit and educating subject on proper dosing regimen

· o Accurate and timely completion of source documents recording subject’s participation in study

· o Communicate closely with all departments to ensure study visits are coordinated in compliance with protocol and GCP guidelines

· o Assist investigators in collection of information from study subjects regarding AEs, concomitant medications and other changes throughout participation

· o Responsible for subject scheduling, in coordination with Recruiting

· o Responsible for timely data entry and query resolution

· o Timely reporting of study events (SAEs, protocol deviations, etc) to appropriate departments and other outside agencies (Sponsors, CRO’s, etc.)

· o Following subjects through study completion and creating follow-up care plan with physician, study subject and primary care provider;

· Ensuring preparation for and facilitating of all study monitoring visits and following up promptly with monitor follow-up letters

· Prompt and professional communication with sponsors, representatives and other study related parties

· Maintaining professional and appropriate interactions with study subjects, caregivers, sponsors and all other study related personnel, and staff members

· Keeping management informed of study status and any study-related issues

· Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:

At least 1 years of experience working as a Clinical Research Coordinator.
CCRC certification not required, but preferred
Experience in neurology not required, but preferred
Knowledge of “good clinical practices” for clinical research as defined by the Code of Federal Regulations (CFR).
Demonstrate organizational skills to efficiently and effectively manage multiple clinical trials while providing accurate information in a timely manner.
Communicate and work effectively with a diverse team of professionals
Phlebotomy and ECGs experience not required, but preferred
Knowledge of all components of the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, data management, etc.
Demonstrated interpersonal skills to work with physicians, administrators, work colleagues, representatives from sponsors and others to achieve maximum efficiency in reaching and maintaining workplace goals in a professional manner.
Must be self-directed and be able to manage multiple projects and responsibilities.
Computer skills using PC platform computers with proficiency in Excel and Word to enter data and generate correspondence accurately and experience with various EDC platforms
Experience with IRB portals, such as WIRB and Advarra preferred
A critical thinker with strong attention to detail and superb problem-solving abilities.

Compensation: $28-32/h.

Application window will close on June 25th, 2024.

Working Conditions

Indoor, office environment.
Essential physical requirements include sitting, typing, standing, and walking.
Lightly active position, occasional lifting of up to 20 pounds.
Reporting to work, as scheduled, is essential.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.

Job Type: Full-time

Pay: $29.00 - $32.00 per hour

Benefits:

401(k) matching
Dental insurance
Employee discount
Flexible schedule
Health insurance
Health savings account
Life insurance
Paid time off
Vision insurance

Experience:

Clinical research: 1 year (Required)
randomizing patients: 1 year (Required)
conducting patients visits: 1 year (Required)

Ability to Commute:

Englewood, CO 80113 (Required)

Work Location: In person

Quick Apply

Study Manager jobs

Clinical Research Coordinator

Clinical Project Manager – Senior - Information Services Regional Strategic Projects

Clinical Study Manager (USA - REMOTE)

Clinical Research Coordinator I Registered Nurse

Senior Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Site Manager

Clinical Research Coordinator (CRC)-FT

Clinical Study Manager

Clinical Research Nurse Coordinator

Non-Clinical Study Manager

Senior Clinical Data Manager

RN Clinical Research Coordinator

Study Start Up Manager

Clinical Project Manager

Customer Success Manager, Clinical Trials

Looking for Psychiatry Research Coordinator/Sub-Investigator Position

Clinical Research Coordinator (medical research trial coordinator with 1 year experience)

Senior, Clinical Study Manager

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